ENST00000525341.2:c.551G>T
|
|
|
ENST00000528641.7:c.385G>T
|
ENSP00000434982.3:p.Glu129Ter
|
|
ENST00000529797.2:n.1086G>T
|
|
|
ENST00000682324.1:c.468+688G>T
|
ENSP00000508017.1:n.468+688G>T
|
|
ENST00000682659.1:c.205G>T
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ENSP00000507351.1:p.Glu69Ter
|
|
ENST00000682699.1:c.574G>T
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ENSP00000507935.1:p.Glu192Ter
|
|
ENST00000683237.1:c.574G>T
|
ENSP00000507343.1:p.Glu192Ter
|
|
ENST00000683856.1:c.397G>T
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ENSP00000507979.1:p.Glu133Ter
|
|
ENST00000684006.1:c.574G>T
|
ENSP00000507269.1:p.Glu192Ter
|
|
ENST00000684657.1:c.394G>T
|
ENSP00000507961.1:p.Glu132Ter
|
|
ENST00000279146.8:c.574G>T
MANE Select
|
ENSP00000279146.3:p.Glu192Ter
|
|
ENST00000279146.7:c.574G>T
|
ENSP00000279146.3:p.Glu192Ter
|
|
ENST00000525341.1:c.226G>T
|
ENSP00000476993.1:p.Glu76Ter
|
|
ENST00000528641.6:c.385G>T
|
ENSP00000434982.2:p.Glu129Ter
|
|
NM_001302959.1:c.397G>T
|
NP_001289888.1:p.Glu133Ter
|
|
NM_001302960.1:c.574G>T
|
NP_001289889.1:p.Glu192Ter
|
|
NM_003977.3:c.574G>T
|
NP_003968.3:p.Glu192Ter
|
|
XM_024448761.1:c.574G>T
|
XP_024304529.1:p.Glu192Ter
|
|
NM_003977.4:c.574G>T
MANE Select
|
NP_003968.3:p.Glu192Ter
|
|
NM_001302960.2:c.574G>T
|
NP_001289889.1:p.Glu192Ter
|
|
NM_001302959.2:c.397G>T
|
NP_001289888.1:p.Glu133Ter
|
|